FDA UDI In Commercial Distribution 🇺🇸 United States

SURGISTAR

DI: 00878799002310 · Model: 7536 · SURGISTAR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURGISTAR
Primary DI
00878799002310
Version / Model
7536
Company Name
SURGISTAR, INC.
Labeler DUNS
808865125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-08
Public Version
3
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
c65b3c59-dfa2-400f-860b-bb9f82d428e8

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EMF Knife, Surgical

GMDN Terms

Code Name
47569 Scalpel, single-use

Identifiers

Type ID
Package 10878799002317
Primary 00878799002310

Customer Contacts

Phone
17605982480